David Bourget (Western Ontario)
David Chalmers (ANU, NYU)
Rafael De Clercq
Jack Alan Reynolds
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Science and Engineering Ethics 12 (1):175-183 (2006)
Almost all ethical guidelines and legislative policies concerning biomedical research involving human subjects contain provisions about relevance of research for the participating populations, informed consent, adequate care for research induced injuries and several other safeguards but the poor continue to suffer. Globalization has further aggravated poor people’s vulnerability by exposing them to international markets. Since the developing countries are abode of higher population of the poor they have become the unholy mines of this human ore for researchers. In this paper I examine various dimensions of poverty and analyze the international ethical responses in the area of biomedical research involving human subjects in order to determine their adequacy to protect the poor against exploitation and misuse and conclude that in view of the poor’s inherent and extreme vulnerability and the failure of ethical pronouncements to protect them from misuse and exploitation, they should be excluded from being enrolled as research subjects.
|Keywords||research poor vulnerability inducement exploitation exclusion|
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References found in this work BETA
Rogeer Hoedemaekers & Henk ten Have (1998). Commercialisation of Genetic Diagnostic Services. Medicine, Health Care and Philosophy 1 (3):217-224.
Citations of this work BETA
Ben Fraser (2013). The Reluctant Mercenary: Vulnerability and the 'Whores of War'. Journal of Military Ethics 12 (3):235-251.
Bette Anton (1999). CQ Sources/Bibliography. Cambridge Quarterly of Healthcare Ethics 8 (04):348-350.
Raymond E. Spier (2006). Conference Summary: 'The Responsible Conduct of Basic and Clinical Research'. Science and Engineering Ethics 12 (1):189-197.
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